Canonical Allele Identifier: CA392100011
Gene: TGM5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43252925A>T , CM000677.2:g.43252925A>T GRCh38
NC_000015.9:g.43545123A>T , CM000677.1:g.43545123A>T GRCh37
NC_000015.8:g.41332415A>T NCBI36
NG_016124.1:g.18933T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000220420.10:c.696T>A MANE Select ENSP00000220420.5:p.Asn232Lys
ENST00000635871.1:n.165T>A
ENST00000220420.9:c.696T>A ENSP00000220420.5:p.Asn232Lys
ENST00000349114.8:c.450T>A ENSP00000220419.8:p.Asn150Lys
ENST00000610827.4:c.693T>A ENSP00000479732.1:p.Asn231Lys
ENST00000611276.4:c.447T>A ENSP00000482542.1:p.Asn149Lys
ENST00000622115.1:c.699T>A ENSP00000479638.1:p.Asn233Lys
NM_004245.3:c.450T>A NP_004236.1:p.Asn150Lys
NM_201631.3:c.696T>A NP_963925.2:p.Asn232Lys
XM_011522229.1:c.696T>A XP_011520531.1:p.Asn232Lys
XR_931948.1:n.870T>A
NM_004245.4:c.450T>A NP_004236.1:p.Asn150Lys
NM_201631.4:c.696T>A MANE Select NP_963925.2:p.Asn232Lys